Data / Medical devices / China / Zhejiang Richall Medical Technology Co., Ltd
Zhejiang Richall Medical Technology Co., Ltd: FDA-registered device maker in Jinhua City Zhejiang, China, 2 510(k) clearances
Zhejiang Richall Medical Technology Co., Ltd is registered with the FDA (registration 3031588965) in Jinhua City Zhejiang, China. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated September 5, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3031588965
- Address
- No. 353 Baozhang Avenue, Xianhua Street, Pujiang County, Jinhua City Zhejiang, China, 322299
- Owner or operator
- Zhejiang Richall Medical Technology Co., Ltd (10090806)
- Roles
- Manufacturer
- First device listed
- May 16, 2024
- Registered through
- 2026
- Brand names listed
- Electric wheelchair (N3901), Electric wheelchair (W3902), Walker
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Walker, Mechanical | ITJ | 1 | Manufacturer | accessdata.fda.gov |
| Wheelchair, Powered | ITI | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| September 5, 2024 | K241723 | Electric wheelchair (W3902) | ITI | Substantially Equivalent | Zhejiang Richall Medical Technology Co., Ltd. | accessdata.fda.gov |
| September 5, 2024 | K241721 | Electric wheelchair (N3901) | ITI | Substantially Equivalent | Zhejiang Richall Medical Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated September 5, 2024. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.